Canonical Allele Identifier: PA220448
Gene: GLA HGNC NCBI

Linked Data

ClinVar Variation Id: 92542
ClinVar RCV Id: RCV000078267
ClinVar Variation Id: 495693
ClinVar RCV Id: RCV000588414 RCV001807298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000160.1:p.Trp44Cys
CA021525
NM_000169.3:c.132G>C
CA413937124
NM_000169.3:c.132G>T